To assess the efficacy and safety of pre-operative capecitabine and oxaliplatin followed by capecitabine with concurrent radiotherapy followed by post-operative capecitabine in the treatment of patients with locally advanced or inoperable rectal cancer.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
109
Pathological complete response rate.
Acute toxicity has been evaluated in previous phase I studies and should occur to a similar extent.
Progression-free survival
Treatment related toxicity
Overall survival
Radiological response rate
Proportion of patients achieving pathological down staging compared with the pre-treatment MRI scan
Surgical complications
Bowel function and quality of life
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.